Acetic Anhydride → 9-Decenyl acetate

HRID 1090465Notes

Reaction equation

HRID 1090465 reaction equation
[C:1]([O:4][C:5](=[O:7])[CH3:6])(=O)[CH3:2].[CH2:8](O)[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15]C=C>CS(O)(=O)=O>[C:5]([O:4][CH2:1][CH2:2][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH:9]=[CH2:8])(=[O:7])[CH3:6]

Participants

4

Conditions

Temperature
30 °C

Procedure

Acetic anhydride, 54.0 grams (0.52 mole), was stirred, and one drop (catalyst) of methanesulfonic acid was added. To this was cautiously added dropwise 50.0 grams (0.32 mole) of 9-decen-1-ol. The addition caused an exothermic reaction which warmed the reaction mixture to 30° C. Upon completion of addition, the reaction mixture was warmed to 60° C. where it stirred for 18 hours. The reaction mixture was cooled and poured into 600 ml of ice/water. The mixture was stirred until the ice melted, and then the layers were separated. The aqueous layer was washed with one 300 ml portion of diethyl ether. The wash was combined with the organic layer, and the combination was washed repeatedly with aqueous 1N sodium hydroxide until the organic layer was basic. The organic layer was dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to a residual oil. The oil was distilled under reduced pressure, yielding 57 grams of 9-decenyl acetate; b.p. 93°-95° C./1.5 mm. The nmr spectrum was consistent with the proposed structure.

Workup

  1. additionThe addition
  2. customan exothermic reaction which
  3. additionUpon completion of addition
  4. temperaturethe reaction mixture was warmed to 60° C. where it
  5. temperatureThe reaction mixture was cooled
  6. customthe layers were separated
  7. washThe aqueous layer was washed with one 300 ml portion of diethyl ether
  8. washthe combination was washed repeatedly with aqueous 1N sodium hydroxide until the organic layer
  9. dry with materialThe organic layer was dried with sodium sulfate
  10. filtrationfiltered
  11. concentrationThe filtrate was concentrated under reduced pressure to a residual oil
  12. distillationThe oil was distilled under reduced pressure

Sources & evidence

ORD record
ord-7ba171de7ed74477b6619762df302ef9
Source dataset
uspto-grants-1992_01
Patent number
US05081287

Reaction notes

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